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J Med Genet. 1987 November; 24(11): 659–663.
PMCID: PMC1050342

Hypohidrotic ectodermal dysplasia.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • LYON MF. Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature. 1961 Apr 22;190:372–373. [PubMed]
  • Stevenson AC, Kerr CB. On the distribution of frequencies of mutation to genes determining harmful traits in man. Mutat Res. 1967 May-Jun;4(3):339–352. [PubMed]
  • Davis JR, Solomon LM. Cellular immunodeficiency in anhidrotic ectodermal dysplasia. Acta Derm Venereol. 1976;56(2):115–120. [PubMed]
  • Söderholm AL, Kaitila I. Expression of X-linked hypohidrotic ectodermal dysplasia in six males and in their mothers. Clin Genet. 1985 Aug;28(2):136–144. [PubMed]
  • Clouston HR. THE MAJOR FORMS OF HEREDITARY ECTODERMAL DYSPLASIA : (With an Autopsy and Biopsies on the Anhydrotic Type). Can Med Assoc J. 1939 Jan;40(1):1–7. [PMC free article] [PubMed]
  • Mills J. Anhidrotic ectodermal dysplasia presenting as a pyrexia of undertermined origin in the neonatal period. Postgrad Med J. 1968 Feb;44(508):193–194. [PMC free article] [PubMed]
  • Salisbury DM, Stothers JK. Hypohidrotic ectodermal dysplasia and sudden infant death. Lancet. 1981 Jan 17;1(8212):153–154. [PubMed]
  • Pabst HF, Groth O, McCoy EE. Hypohidrotic ectodermal dysplasia with hypothyroidism. J Pediatr. 1981 Feb;98(2):223–227. [PubMed]
  • Passarge E, Fries E. Autosomal recessive hypohidrotic ectodermal dysplasia with subclinical manifestation in the heterozygote. Birth Defects Orig Artic Ser. 1977;13(3C):95–100. [PubMed]
  • Pinheiro M, Ideriha MT, Chautard-Freire-Maia EA, Freire-Maia N, Primo-Parmo SL. Christ-Siemens-Touraine syndrome. Investigations on two large Brazilian kindreds with a new estimate of the manifestation rate among carriers. Hum Genet. 1981;57(4):428–431. [PubMed]
  • Nakata M, Koshiba H, Eto K, Nance WE. A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia. Am J Hum Genet. 1980 Nov;32(6):908–919. [PubMed]
  • Kleinebrecht J, Degenhardt KH, Grubisic A, Günther E, Svejcar J. Sweat pore counts in ectodermal dysplasias. Hum Genet. 1981;57(4):437–439. [PubMed]
  • Filippi G, Rinaldi A, Crisponi G, Daniels GL, Siniscalco M. X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency. J Med Genet. 1979 Jun;16(3):223–224. [PMC free article] [PubMed]
  • Gerald PS, Brown JA. Proceedings: Report of the Committee on the Genetic Constitution of the X Chromosome. Cytogenet Cell Genet. 1974;13(1):29–34. [PubMed]
  • MacDermot KD, Winter RM, Malcolm S. Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome). Hum Genet. 1986 Oct;74(2):172–173. [PubMed]

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